SPRYD7

SPRYD7
Identifiers
Aliases	SPRYD7, C13orf1, CLLD6, SPRY domain containing 7
External IDs	OMIM: 607866; MGI: 1913924; HomoloGene: 10725; GeneCards: SPRYD7; OMA:SPRYD7 - orthologs
Gene location (Human)
Chr.	Chromosome 13 (human)
End	49,936,490 bp
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)
End	61,794,335 bp
RNA expression pattern
	Top expressed in
	gastrocnemius muscle; ; muscle of thigh; ; gonad; ; dorsolateral prefrontal cortex; ; Brodmann area 9; ; cingulate gyrus; ; anterior cingulate cortex; ; endothelial cell; ; middle temporal gyrus; ; right frontal lobe;
	Top expressed in
	dorsomedial hypothalamic nucleus; ; ventral tegmental area; ; spermatocyte; ; triceps brachii muscle; ; habenula; ; paraventricular nucleus of hypothalamus; ; temporal muscle; ; sternocleidomastoid muscle; ; dorsal tegmental nucleus; ; lateral septal nucleus;
	More reference expression data
	More reference expression data
Orthologs
	57213
	66674
	ENSG00000123178
	ENSMUSG00000021930
	Q5W111
	Q3TFQ1
	NM_001127482; NM_020456
	NM_025697; NM_001310603
	NP_001120954; NP_065189
	NP_001297532; NP_079973
	Wikidata
View/Edit Human	View/Edit Mouse

SPRY domain-containing protein 7 (SPRYD7) also known as chronic lymphocytic leukemia deletion region gene 6 protein (CLLD6) is a protein that in humans is encoded by the SPRYD7 gene.^[5]^[6]^[7]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000123178 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000021930 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Mabuchi H, Fujii H, Calin G, Alder H, Negrini M, Rassenti L, Kipps TJ, Bullrich F, Croce CM (Apr 2001). "Cloning and characterization of CLLD6, CLLD7, and CLLD8, novel candidate genes for leukemogenesis at chromosome 13q14, a region commonly deleted in B-cell chronic lymphocytic leukemia". Cancer Res. 61 (7): 2870–7. PMID 11306461.
^ Tiazhelova TV, Ivanov DV, Makeeva NV, Kapanadze BI, Nikitin EA, Semov AB, Sangfeldt O, Grander D, Vorob'ev AI, Einhorn S, Iankovskii NK, Baranova AV (Dec 2001). "[Transcription map of the 13q14 region, frequently deleted in B-cell chronic lymphocytic leukemia patients]". Genetika. 37 (11): 1530–7. PMID 11771308.
^ "Entrez Gene: C13orf1 chromosome 13 open reading frame 1".

Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction". Anal. Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.
Yu W, Andersson B, Worley KC, et al. (1997). "Large-Scale Concatenation cDNA Sequencing". Genome Res. 7 (4): 353–8. doi:10.1101/gr.7.4.353. PMC 139146. PMID 9110174.
Mertens D, Wolf S, Schroeter P, et al. (2002). "Down-regulation of candidate tumor suppressor genes within chromosome band 13q14.3 is independent of the DNA methylation pattern in B-cell chronic lymphocytic leukemia". Blood. 99 (11): 4116–21. doi:10.1182/blood.V99.11.4116. PMID 12010815.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801. S2CID 23783563.
Dunham A, Matthews LH, Burton J, et al. (2004). "The DNA sequence and analysis of human chromosome 13". Nature. 428 (6982): 522–8. Bibcode:2004Natur.428..522D. doi:10.1038/nature02379. PMC 2665288. PMID 15057823.
Gerhard DS, Wagner L, BB Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.

This article on a gene on human chromosome 13 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000123178 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000021930 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid11306461-5] Mabuchi H, Fujii H, Calin G, Alder H, Negrini M, Rassenti L, Kipps TJ, Bullrich F, Croce CM (Apr 2001). "Cloning and characterization of CLLD6, CLLD7, and CLLD8, novel candidate genes for leukemogenesis at chromosome 13q14, a region commonly deleted in B-cell chronic lymphocytic leukemia". Cancer Res. 61 (7): 2870–7. PMID 11306461.

[pmid11771308-6] Tiazhelova TV, Ivanov DV, Makeeva NV, Kapanadze BI, Nikitin EA, Semov AB, Sangfeldt O, Grander D, Vorob'ev AI, Einhorn S, Iankovskii NK, Baranova AV (Dec 2001). "[Transcription map of the 13q14 region, frequently deleted in B-cell chronic lymphocytic leukemia patients]". Genetika. 37 (11): 1530–7. PMID 11771308.

[entrez-7] "Entrez Gene: C13orf1 chromosome 13 open reading frame 1".

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[7]

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[2]

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SPRYD7

References

Further reading